Stem cells and Bronchopulmonary Dysplasia - The five questions: Which cells, when, in which dose, to which patients via which route?

被引:11
|
作者
Mueller, Martin [1 ,2 ,3 ]
Kramer, Boris W. [4 ,5 ,6 ]
机构
[1] Univ Hosp Bern, Dept Obstet & Gynecol, Bern, Switzerland
[2] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT USA
[3] Univ Bern, Dept Clin Res, Bern, Switzerland
[4] Maastricht Univ, Med Ctr, MUMC, Dept Pediat, Maastricht, Netherlands
[5] Maastricht Univ, Sch Mental Hlth & Neurosci, Maastricht, Netherlands
[6] Sch Oncol & Dev Biol GROW, Maastricht, Netherlands
关键词
Bronchopulmonary dysplasia; mesenchymal stem cell transplantation; paracrine immunomodulation; physiologic actions; outcomes; MESENCHYMAL PROGENITOR CELLS; CHRONIC LUNG-DISEASE; STROMAL CELLS; PRETERM BIRTH; LONG-TERM; INJURY; THERAPY; DIFFERENTIATION; PROLIFERATION; INFLAMMATION;
D O I
10.1016/j.prrv.2016.12.003
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Preterm birth is the leading cause of death in newborns and children. Despite advances in perinatology, immature infants continue to face serious risks such chronic respiratory impairment from bronchopulmonary dysplasia (BPD). Current treatment options are insufficient and novel approaches are desperately needed. In recent years stem cells have emerged as potential candidates to treat BPD with mesenchymal stemistromal cells (MSCs) being particularly promising. MSCs originate from several stem cell niches including bone marrow, skin, or adipose, umbilical cord, and placental tissues. Although the first MSCs clinical trials in BPD are ongoing, multiple questions remain open. In this review, we discuss the question of the optimal cell source (live cells or cell products), route and timing of the transplantation. Furthermore, we discuss MSCs possible capacities including migration, homing, pro-angiogenesis, anti-inflammatory, and tissue-regenerative potential as well. (C) 2016 Published by Elsevier Ltd.
引用
收藏
页码:54 / 59
页数:6
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